Cook Medical recalled the Thal-Quick Chest Tube Tray, reference part number C-TQTSY-3200, Order G07242, due to expiration dates that exceed true shelf life. The recall is active and worldwide. The hazard is labeling that misstates shelf life. Patients and healthcare providers should stop using the affected devices immediately and follow Cook’s recall instructions.
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Cook Incorporated or your healthcare provider for instructions. Notification method: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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The Thal-Quick Chest Tube Tray is a surgical accessory used in chest drainage procedures. It is distributed worldwide and intended for healthcare facilities.
Expiration date labels that exceed the true shelf life could lead to use of outdated sterile or effective devices, potentially compromising sterility and patient safety.
This recall is not described as part of a broader industry pattern in the provided notice.
UDI and lot numbers are typically printed on the device packaging or accompanying labels.
Refunds or replacements are coordinated by Cook Medical; timelines vary by recall instructions.
Keep the recall notice, product packaging, lot numbers, and any correspondence with Cook Medical as records.
Product: Thal-Quick Chest Tube Tray. Reference Part Number: C-TQTSY-3200. UDI: 01)00827002072428(17)270221(10)NS15796862X and 01)00827002072428(17)270301(10)NS15881832X. Lot Numbers: NS15796862X, NS15881832X. Quantity: 2 units. Distribution: Worldwide. Recall Date: 2026-03-05. Status: ACTIVE.
No injuries or incidents have been reported.
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Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.